Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k) Clearances

510(k) cleared devices tracked by MedTracker

CIG 1981-10-20

BECKMAN ASTRA SYS. TOTAL BILIRUBIN MOD

Applicant Beckman Instruments, Inc.

K-Number K812784

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DSH 1981-10-20

ECG MEDATAPE-601

Applicant Hospital Equipment Service

K-Number K812763

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CET 1981-10-20

LIPASE

Applicant Pointe Scientific, Inc.,

K-Number K812794

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DRS 1981-10-20

PHYSIOLOGICAL PRESSURE TRANSDUCER

Applicant Electromedics, Inc.

K-Number K812758

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GDY 1981-10-20

X-RAY DETECTABLE LAP SPONGES

Applicant Procter & Gamble Mfg. Co.

K-Number K812651

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HGM 1981-10-20

MODEL AP 180 MINI-MONITOR

Applicant Sonicaid, Inc.

K-Number K812256

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JIX 1981-10-19

BECKMAN ICS CALIBRATOR

Applicant Beckman Instruments, Inc.

K-Number K812649

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FJS 1981-10-19

CUFF MATERIAL ON PEDIATRIC SIZE CATH.

Applicant Quinton, Inc.

K-Number K812718

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HNN 1981-10-19

ADJUSTABLE MICROSURGICAL KNIFE

Applicant Vxtra Corp.

K-Number K812620

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HHD 1981-10-19

UNSCENTED MENSTRUAL PADS

Applicant Weyerhaeuser Co.

K-Number K812577

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FKO 1981-10-19

NON-STERILE SHADOW-STRIPE CATHETER

Applicant Quinton, Inc.

K-Number K812717

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FEM 1981-10-19

POLAROID INSTANT ENDOCAMERA

Applicant Polaroid Corp.

K-Number K812542

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